Special

GgaINT0127352 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr18:1044026-1044562:+
Coord C1 exon
chr18:1044026-1044058
Coord A exon
chr18:1044059-1044435
Coord C2 exon
chr18:1044436-1044562
Length
377 bp
Sequences
Splice sites
5' ss Seq
TGAATAAGA
5' ss Score
-3.07
3' ss Seq
CATTCACTTTGTTTCTCCAGGCT
3' ss Score
8.83
Exon sequences
Seq C1 exon
GCTTCACAAACACAAAGAGATGACTAGGTTTGA
Seq A exon
ATAAGACTTTAAAATACAGCTTGTTAAAATAAAAGCAGTTATAGAAACTTTCATCCCAGTGTGAAATCACCTGTGAAAATTATGAACTTGTCTAAAACAGCAAGTCAGACTGCAAATGCTTTCCAGCTTCTTCCACTTCTGGTTTTGCTTTTTCATGAGGCTCCTGGGCTATTTGGCCCTTGGGGATACAGGGAGACCCGTGAGTTACTACATGCTATGCTGCCCTATTCAGTGAATGCTGTTGAGGACCACACCGTAGGCCCAGCTCATGCCTGACACTCTCCCATGGCAAAGGAGAATCTGCCCAACTGCAGCATGGAGCATGAGGGGATATTCTTCTGCCTGTCCTGTGCTGTTCATTCACTTTGTTTCTCCAG
Seq C2 exon
GCTGTCACTGTGTGAGAAGGCTTTGGCTGAATATTTGGACAGGAAGAGGTTGGCCTTTCCCAGATTTTACTTCATTTCTTCTGCAGATTTATTGGATATTCTTTCCAATGGCACCAACCCACAGCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001111:ENSGALT00000039398:22
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF083938=DHC_N2=FE(2.1=100)
A:
NA
C2:
PF083938=DHC_N2=FE(10.0=100)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]